Canonical Allele Identifier: CA147890850
Gene: ARG1 HGNC NCBI

Linked Data

dbSNP Id: rs573069792

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131573153A>G , CM000668.2:g.131573153A>G GRCh38
NC_000006.11:g.131894293A>G , CM000668.1:g.131894293A>G GRCh37
NC_000006.10:g.131935986A>G NCBI36
NG_007086.2:g.4929A>G
NG_031860.1:g.60071T>C
NG_031860.2:g.60071T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000672052.1:n.305-3510A>G
ENST00000672233.1:c.77-5958A>G ENSP00000499826.1:n.77-5958A>G
ENST00000673234.1:c.77-3510A>G ENSP00000499885.1:n.77-3510A>G
ENST00000368087.7:c.-130A>G ENSP00000357066.3:n.-130A>G